Siemens recalls Uroskop Omnia Max diagnostic imaging systems with software VE10 & VF11 due to potential collision risks with walls or ceilings that could cause serious injury to staff or patients.
Potential risk of collision with the ceiling, wall, or objects which may result in serious injury to staff or patients due to room configuration parameters of the system being set to default values
Siemens is recalling Uroskop Omnia Max diagnostic imaging systems with software VE10 and VF11 because default room configuration settings could cause the device to collide with walls or ceilings, potentially injuring staff or patients. This is a serious safety issue that requires immediate attention.
The system's default room configuration settings may cause it to collide with walls, ceilings, or objects. This collision could result in serious injury to staff or patients during medical procedures.
Healthcare facilities using Siemens Uroskop Omnia Max systems with software VE10 or VF11 are affected. Staff and patients in rooms where the device is installed are at the highest risk of injury.
Check for the model number 10762473 on the device. The system was sold with software versions VE10 or VF11. Serial numbers listed in the recall include a long sequence of numbers starting with 4645.
Immediately stop using the Uroskop Omnia Max system with software VE10 or VF11 to prevent potential collisions.
Software versions VE10 and VF11.
Check the model number (10762473) and software version on your device. The serial numbers listed in the recall include a specific sequence of numbers starting with 4645.
The recall record does not mention a fix or remedy.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1168-2023 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1168-2023 from Siemens. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
